Suppr超能文献

神经退行性疾病中的蛋白质修饰

Protein modification in neurodegenerative diseases.

作者信息

Ramazi Shahin, Dadzadi Maedeh, Darvazi Mona, Seddigh Nasrin, Allahverdi Abdollah

机构信息

Department of Biophysics Faculty of Biological Sciences Tarbiat Modares University Tehran Iran.

Department of Biotechnology Faculty of Advanced Science and Technology Tehran Medical Sciences Islamic Azad University Tehran Iran.

出版信息

MedComm (2020). 2024 Aug 4;5(8):e674. doi: 10.1002/mco2.674. eCollection 2024 Aug.

Abstract

Posttranslational modifications play a crucial role in governing cellular functions and protein behavior. Researchers have implicated dysregulated posttranslational modifications in protein misfolding, which results in cytotoxicity, particularly in neurodegenerative diseases such as Alzheimer disease, Parkinson disease, and Huntington disease. These aberrant posttranslational modifications cause proteins to gather in certain parts of the brain that are linked to the development of the diseases. This leads to neuronal dysfunction and the start of neurodegenerative disease symptoms. Cognitive decline and neurological impairments commonly manifest in neurodegenerative disease patients, underscoring the urgency of comprehending the posttranslational modifications' impact on protein function for targeted therapeutic interventions. This review elucidates the critical link between neurodegenerative diseases and specific posttranslational modifications, focusing on Tau, APP, α-synuclein, Huntingtin protein, Parkin, DJ-1, and Drp1. By delineating the prominent aberrant posttranslational modifications within Alzheimer disease, Parkinson disease, and Huntington disease, the review underscores the significance of understanding the interplay among these modifications. Emphasizing 10 key abnormal posttranslational modifications, this study aims to provide a comprehensive framework for investigating neurodegenerative diseases holistically. The insights presented herein shed light on potential therapeutic avenues aimed at modulating posttranslational modifications to mitigate protein aggregation and retard neurodegenerative disease progression.

摘要

翻译后修饰在调控细胞功能和蛋白质行为方面发挥着关键作用。研究人员已将失调的翻译后修饰与蛋白质错误折叠联系起来,而蛋白质错误折叠会导致细胞毒性,尤其是在诸如阿尔茨海默病、帕金森病和亨廷顿病等神经退行性疾病中。这些异常的翻译后修饰会使蛋白质在大脑中与疾病发展相关的特定部位聚集。这会导致神经元功能障碍以及神经退行性疾病症状的出现。认知能力下降和神经损伤在神经退行性疾病患者中普遍存在,这凸显了理解翻译后修饰对蛋白质功能的影响以进行靶向治疗干预的紧迫性。本综述阐明了神经退行性疾病与特定翻译后修饰之间的关键联系,重点关注tau蛋白、淀粉样前体蛋白(APP)、α-突触核蛋白、亨廷顿蛋白、帕金森蛋白、DJ-1蛋白和动力相关蛋白1(Drp1)。通过描述阿尔茨海默病、帕金森病和亨廷顿病中突出的异常翻译后修饰,本综述强调了理解这些修饰之间相互作用的重要性。本研究着重介绍10种关键的异常翻译后修饰,旨在提供一个全面的框架,以便从整体上研究神经退行性疾病。本文提出的见解揭示了潜在的治疗途径,旨在调节翻译后修饰以减轻蛋白质聚集并延缓神经退行性疾病的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6712/11298556/feb028a60a6f/MCO2-5-e674-g002.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验